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congenital urachal anomaly - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

congenital urachal anomaly

MONDO:0018565

Overview

Congenital urachal anomaly (CUA) describes a group of urachal remnants, found more frequently in males than females, that result from incomplete closure of the urachus (an embryological remnant of the allantois) during prenatal development, and that are usually asymptomatic (and found as an incidental finding on a radiological study) but can also present with umbilical discharge (in patent urachus or urachal sinus), infraumblical mass and pain, or with complications such as obstruction and infection. CUAs include patent urachus, urachal sinus, urachal cyst and urachal diverticulum.

ResearchLimited published research (5 articles)

Research Landscape

Sourced from ClinicalTrials.gov and PubMed. Publication types are classified using NLM-curated article metadata; research type breakdowns reflect the nature of published work for this disease.

No clinical trials have been registered for congenital urachal anomaly.

5 publications have been identified in PubMed for congenital urachal anomaly. Research spans Case Report / Case Series (100%).

Recent Publications

Alzahrani HM (2025). [PMID: 40636335](https://pubmed.ncbi.nlm.nih.gov/40636335/). *Clin Case Rep*. [Case Report / Case Series]
Murshid MY (2025). [PMID: 40453746](https://pubmed.ncbi.nlm.nih.gov/40453746/). *J Surg Case Rep*. [Case Report / Case Series]
Javed E (2025). [PMID: 40787160](https://pubmed.ncbi.nlm.nih.gov/40787160/). *Clin Case Rep*. [Case Report / Case Series]
Akshitha E (2025). [PMID: 40199592](https://pubmed.ncbi.nlm.nih.gov/40199592/). *BMJ Case Rep*. [Case Report / Case Series]
Watkins-Granville NM (2024). [PMID: 39479082](https://pubmed.ncbi.nlm.nih.gov/39479082/). *Cureus*. [Case Report / Case Series]

Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 7:55 PM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:435743

GARD

Genetic and Rare Diseases Info Center

GARD:21814

Questions for Your Care Team

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congenital urachal anomaly

Overview

Research Landscape

Recent Publications

Medical References

External Resources

Orphanet

GARD

Related Diseases

Questions for Your Care Team

Questions for Your Care Team